N-(2-(2-Hydroxyethylamino)ethyl)cholesteryl-3-carboxamide (OH-Chol) and OH-C-Chol were synthesized as previously described (17). Cholesteryl (3-((2-hydroxyethyl)amino)propyl)carbamate hydroiodide (HAPC-Chol) and cholesteryl (3-((2-hydroxyethyl)(methyl)amino)propyl)carbamate hydroiodide (MHAPC-Chol), were also synthesized as previously described (18). 1,2-Dioleoyl-3-trimethyl-ammonium-propane methyl sulfate salt (DOTAP) was obtained from Avanti Polar Lipids, Inc. (Alabaster, AL, USA). N,N-Dimethyl-N-octade-cyloctadecan-1-aminium bromide [DC-1-18, also known as dimethyldioctadecylammonium bromide (DDAB)] and 11-((1,3-bis (dodecanoyloxy)-2-((dodecanoyloxy)methyl)propan-2-yl)amino)-N,N,N-trimethyl-11-oxoundecan-1-aminium bromide (TC-1-12) were obtained from Sogo Pharmaceutical Co., Ltd. (Tokyo, Japan). The lipid names of the DC- and TC-series are product names of Sogo Pharmaceutical Co., Ltd. DOPE and N-(methyl-poly-oxyethylene oxycarbonyl)-1,2-distearoyl-sn-glycero-3-phosphoethanolamine, sodium salt (PEG₂₀₀₀-DSPE, SUNBRIGHT^® DSPE-020CN) were obtained from NOF Co. Ltd. (Tokyo, Japan).

siRNAs targeting nucleotides of Firefly luciferase (Luc siRNA), non-silencing siRNA [control (Cont) siRNA] as a negative control for Luc siRNA, apolipoprotein B siRNA (ApoB siRNA), luciferase siRNA (Cont siRNA) as a negative control for ApoB siRNA, cyanine 5.5 (Cy5.5)-labeled pGL3 luciferase siRNA (Cy5.5-siRNA) were synthesized by Sigma Genosys (Tokyo, Japan). Mouse Tie2 siRNA and luciferase siRNA (Cont siRNA) as a negative control for Tie2 siRNA were synthesized by Japan Bio Services Co., Ltd. (Saitama, Japan). The siRNA sequences of the Luc siRNA were as reported previously (19). Cy5.5-siRNA and Cont siRNA as a negative control for Luc siRNA were as reported previously (20). ApoB siRNA and Cont siRNA as a negative control for ApoB siRNA were conjugated with cholesterol at the 3'-end of the sense strand, and the siRNA sequences were as reported previously (21). Tie2 siRNA and Cont siRNA as a negative control for Tie2 siRNA were blunt-ended, alternating 2'-O-methyl-modified siRNA, and the siRNA sequences were as reported previously (16, 22).

The cationic cholesterol derivative-based liposomes were prepared from OH-Chol/DOPE (composition designated as LP-OH), OH-C-Chol/DOPE (composition designated as LP-OH-C), HAPC-Chol/DOPE (composition designated as LP-HAPC) and MHAPC-Chol/DOPE (composition designated as LP-MHAPC), at a molar ratio of 3:2. Cationic liposomes, including dialkyl or trialkyl cationic lipids were prepared from DOTAP/DOPE (composition designated as LP-DOTAP), DC-1-18/DOPE (composition designated as LP-DC-1-18), and TC-1-12/DOPE (composition designated as LP-TC-1-12), at a molar ratio of 1:1. PEGylated cationic liposomes were incorporated with 1 mol% PEG₂₀₀₀-DSPE into each liposomal formulation.

For the preparation of cationic liposomes and PEGylated cationic liposomes using a thin-film hydration method, cationic lipid, DOPE and PEG₂₀₀₀-DSPE were dissolved in chloroform, and chloroform was evaporated under vacuum in a rotary evaporator at 60˚C to obtain a thin film. The thin film was hydrated with water at 60˚C by vortex mixing. The liposomes were sonicated in a bath-type sonicator (Bransonic^® 2510J-MTH, 100W; Branson UL Trasonics Co., CT, USA) for 5-10 min at room temperature.

To prepare cationic liposome/siRNA complexes (lipoplexes), each cationic liposome was added to 50 pmol siRNA at a charge ratio (+:-) of 7:1 for cationic liposomes composed of cationic cholesterol derivatives and DOPE (17) or 4:1 for cationic liposomes composed of dialkyl or trialkyl cationic lipids and DOPE (23) with vortex-mixing for 10 sec and left at room temperature for 15 min. The charge ratio (+:-) of liposomes:siRNA is expressed as the molar ratio of cationic lipid to siRNA phosphate.

The particle size distributions of non-PEGylated and PEGylated cationic liposomes and lipoplexes were measured by the cumulant method using a light-scattering photometer (ELS-Z2; Otsuka Electronics Co., Ltd., Osaka, Japan) at 25˚C after diluting the dispersion to an appropriate volume with water. The ζ-potentials were measured using electrophoresis light-scattering methods with the ELS-Z2 at 25˚C after diluting the dispersion with an appropriate volume of water.

Human breast cancer MCF-7-Luc cells stably expressing Firefly luciferase by the transfection of plasmid pcDNA3 containing the Firefly luciferase (hLuc) gene from plasmid psiCHECK2 (Promega, Madison, WI, USA) were donated by Dr Kenji Yamato (University of Tsukuba, Tsukuba, Japan). MCF-7-Luc cells were grown in RPMI-1640 medium, supplemented with 10% heat-inactivated fetal bovine serum (FBS) and 1.2 mg/ml G418 at 37˚C in a 5% CO₂ humidified atmosphere.

MCF-7-Luc cells were seeded in 6-well culture plate at a density of 3x10⁵ cells per well 24 h prior to transfection. Non-PEGylated and PEGylated cationic lipoplexes were formed by the addition of non-PEGylated and PEGylated cationic liposomes, respectively, into 50 pmol Cont siRNA or Luc siRNA at the indicated charge ratios (+:-) with vortex-mixing for 10 sec, and left at room temperature for 15 min. For transfection, each cationic lipoplex was diluted in 1 ml of medium supplemented with 10% FBS and the mixture was then added to the cells (50 pmol siRNA/well). At 48 h following transfection, the luciferase activity was measured as counts per sec (cps)/µg protein using the luciferase assay system (Pica Gene; Toyo Ink Mfg. Co. Ltd., Tokyo, Japan) and BCA reagent (Pierce, Rockford, IL, USA), as reported previously (17). Luciferase activity (%) was calculated as relative to the luciferase activity (cps/µg protein) of untransfected cells.

MCF-7-Luc cells were seeded in 96-well plates 24 h prior to transfection. Each cationic lipoplex with 50 pmol Cont siRNA was diluted in 1 ml of medium supplemented with 10% FBS, and the mixture (100 µl) was then added to the cells at 50% confluency in the well (final 50 nM siRNA concentration). Following a 24-h incubation period, cell numbers were determined using a Cell Counting kit-8 (Dojindo Laboratories, Kumamoto, Japan). Cell viability was expressed as relative to the absorbance at 450 nm of untransfected cells.

One female BALB/c mouse (weighing 18-20 g, 8 weeks of age; Sankyo Labo Service Corp., Tokyo, Japan) was housed in a temperature- (24˚C) and humidity- (55%) controlled room with a 12 h light/dark cycle (lights on at 8:00 a.m.) with ad libitum access to food and water. Blood (0.5 ml) was collected from the carotid artery of the mouse while under anesthesia by an intraperitoneal injection of 50 mg/kg body weight of pentobarbital (Nembutal; Dainippon Pharmaceutical Co., Ltd., Osaka, Japan). Erythrocytes were collected from the whole blood at 4˚C by centrifugation at 300 x g for 3 min and resuspended in PBS as a 2% (v/v) suspension of erythrocytes. Non-PEGylated and PEGylated cationic lipoplexes with 2 µg siRNA were added to 100 µl of 2% (v/v) erythrocyte suspension. Following incubation for 15 min at 37˚C, the sample was placed on a glass plate and agglutination was observed using an ECLIPSE TS100-F microscope (Nikon, Tokyo, Japan).

All animal experiments were conducted in accordance with the ‘Guide for the Care and Use of Laboratory Animals’ adopted by the Institutional Animal Care and Use Committee of Hoshi University (Tokyo, Japan) (which is accredited by the Ministry of Education, Culture, Sports, Science, and Technology, Japan). Ethical approval for this study was obtained from the Institutional Animal Care and Use Committee of Hoshi University (Permission no. 29-049).

Non-PEGylated and PEGylated cationic lipoplexes were formed by the addition of non-PEGylated and PEGylated cationic liposomes, respectively, into 20 µg of Cy5.5-siRNA with vortex-mixing for 10 sec and left at room temperature for 15 min. The non-PEGylated or PEGylated cationic lipoplexes with 20 µg of Cy5.5-siRNA were administered intravenously via the lateral tail vein into a total of 14 female BALB/c mice (weighing 18-20 g, 8 weeks of age; Sankyo Labo Service Corp.) (n=1 for each lipoplex). At 1 h post-injection, the mice were sacrificed. Tissues were frozen on dry ice and cut into 16-µm-thick slices. The localization of Cy5.5-siRNA was examined using an Eclipse TS100-F microscope.

For the observation of the biodistribution of siRNA following the injection of PEGylated DOTAP/cholesterol lipoplexes, PEGylated cationic liposomes were prepared by inclusion of 1, 2, 3 and 5 mol% PEG₂₀₀₀-DSPE into the formulations of DOTAP/cholesterol liposomes (molar ratio of 1:1). The PEGylated cationic lipoplexes with 20 µg of Cy5.5-siRNA were administered intravenously via the lateral tail vein into a total of 4 female BALB/c mice (weighing 18-20 g, 8 weeks of age; Sankyo Labo Service Corp.) (n=1 for each lipoplex). At 1 h after the injection, the mice were sacrificed, and Cy5.5 fluorescent imaging of the tissues was performed using a NightOWL LB981 NC100 system (Berthold Technologies, Bad Wildbad, Germany). In Cy5.5 fluorescent imaging, the excitation and emission filters were set at 630/20 and 680/30 nm, respectively. The exposure time for fluorescence was 5 sec. A grayscale body-surface reference image was collected using a NightOWL LB981 CCD camera (Berthold Technologies). The images were analyzed using IndiGo2 software (version 2.0.1.0; Berthold Technologies) provided with the in vivo imaging system. The tissues after fluorescent imaging were frozen on dry ice and sliced at 16 µm. The localization of Cy5.5-siRNA was examined using an Eclipse TS100-F microscope.

PEGylated cationic lipoplexes were formed by the addition of PEGylated cationic liposomes into 50 µg Cont siRNA or ApoB siRNA with vortex-mixing for 10 sec, and left at room temperature for 15 min. The PEGylated cationic lipoplexes were administered intravenously the via the lateral tail vein into female BALB/c mice (8 weeks of age) (n=4 for each lipoplex).

For the expression level of ApoB mRNA in the liver, the livers were excised from the mice at 48 h following the injection of PEGylated cationic lipoplexes, and total RNA was then isolated using Isogen II (Nippon Gene Co., Ltd., Tokyo, Japan). cDNA was synthesized from total RNA of the liver and then first-strand cDNA was synthesized from 2 µg of total RNA using PrimeScript RTase (Takara Bio, Inc., Otsu, Japan). Reverse transcription-quantitative PCR (RT-qPCR) was performed using a Roche Light Cycler 96 system (Roche Diagnostics Ltd., Basel, Switzerland) and TaqMan Gene expression assay (Apob: Mm01545150_m1, gapdh: Mm99999915_g1; Applied Biosystems^®, CA, USA). The thermocycling conditions consisted of an initial denaturation at 95˚C for 600 sec, and 45 cycles of denaturation at 95˚C for 10 sec, and primer annealing and extension at 60˚C for 30 sec (two step amplification). The expression level of ApoB mRNA was normalized using the amount of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA in the same sample, and analyzed using the comparative Cq (2^-ΔΔCq) method (24).

PEGylated cationic lipoplexes were formed by the addition of PEGylated cationic liposomes into 50 µg Cont siRNA or ApoB siRNA with vortex-mixing for 10 sec and left at room temperature for 15 min. PEGylated cationic lipoplexes were administered intravenously via the lateral tail vein into female BALB/c mice (8 weeks of age) (n=4 for each lipoplex). To measure aspartate aminotransferase (AST/GOT) activity, serum was separated from coagulated whole blood at 48 h after the injection. GOT levels in the serum were determined using commercially available test reagents (Transaminase CII-test kit; Wako Pure Chemicals, Osaka, Japan). Normal values were determined using blood obtained from age-matched, untreated female mice (n=4).

PEGylated cationic lipoplexes were formed by the addition of PEGylated cationic liposomes into 50 µg Cont siRNA or Tie2 siRNA with vortex-mixing for 10 sec and left at room temperature for 15 min. The PEGylated cationic lipoplexes were administered intravenously via the lateral tail vein into female BALB/c mice (8 weeks of age) (n=3-4 for each lipoplex). For the expression level of Tie2 mRNA in the lungs, the lungs were excised from the mice at 48 h after the injection of PEGylated cationic lipoplexes, and total RNA was then isolated using Isogen II. cDNA was synthesized from total RNA of the lung, and RT-qPCR was performed using a Roche Light Cycler 96 system and TaqMan Gene expression assays [Tek (Tie-2): Mm00443243_m1, phosphatase and tensin homolog (PTEN): Mm00477208_m1; Applied Biosystems^®]. The thermocycling conditions consisted of an initial denaturation at 95˚C for 600 sec, and 45 cycles of denaturation at 95˚C for 10 sec, and primer annealing and extension at 60˚C for 30 sec (two step amplification). The expression levels of Tie2 mRNA were normalized using the amount of PTEN mRNA in the same sample as reported previously (16) and analyzed using the comparative Cq (2^-ΔΔCq) method.

The statistical significance of differences between mean values was determined by a Student's t-test using GraphPad Prism 4.0 (GraphPad Software Inc., La Jolla, CA, USA). A P-value ≤0.05 was considered to indicate a statistically significant difference.

Firstly, we examined whether the cationic lipid type in cationic liposomes affected in vitro gene silencing. Herein, we used OH-Chol, OH-C-Chol, HAPC-Chol and MHAPC-Chol as cationic cholesterol derivatives; DOTAP and DC-1-18 as dialkyl cationic lipids; and TC-1-12 as a trialkyl cationic lipid for the preparation of cationic liposomes (Fig. 1). We have previously reported that siRNA lipoplexes composed of OH-Chol/DOPE, OH-C-Chol/DOPE, HAPC-Chol/DOPE, MHAPC-Chol/DOPE, DOTAP/DOPE, DC-1-18/DOPE and TC-1-12/DOPE can strongly suppress the expression of a target gene in MCF-7 cells (25). For cationic liposomes with cationic cholesterol derivatives, LP-OH, LP-OH-C, LP-HAPC and LP-MHAPC, were prepared from OH-Chol/DOPE, OH-C-Chol/DOPE, HAPC-Chol/DOPE and MHAPC-Chol/DOPE, respectively, at a molar ratio of 3:2 (Table I) (25). By contrast, for cationic liposomes with dialkyl or trialkyl cationic lipids, LP-DOTAP, LP-DC-1-18, and LP-TC-1-12 were prepared from DOTAP/DOPE, DC-1-18/DOPE and TC-1-12/DOPE, respectively, at a molar ratio of 1:1 (Table I) (25).

The sizes of the cationic liposomes were approximately 80-120 nm, and the ζ-potentials were approximately +42-55 mV (Table I). For the preparation of cationic lipoplexes, cationic liposomes were mixed with siRNA at charge ratios (+:-) of 1:1, 3:1, 5:1 and 7:1 for LP-OH, LP-OH-C, LP-HAPC and LP-MHAPC, and 2:1, 4:1 and 6:1 for LP-DOTAP, LP-DC-1-18 and LP-TC-1-12, respectively. As shown in Table I, LP-OH and LP-OH-C lipoplexes aggregated when they mixed with siRNA at charge ratios (+:-) of 3:1-5:1. By contrast, LP-HAPC and LP-MHAPC lipoplexes aggregated when they mixed with siRNA at charge ratios (+:-) of approximately 3:1 and 1:1, respectively. These results suggested that the cationic charge on the surface of the cationic lipoplexes may be neutralized by the addition of siRNA, resulting in the instability of the lipoplexes. By contrast, the LP-DOTAP, LP-DC-1-18 and LP-TC-1-12 lipoplexes exhibited a positive charge in ζ-potential beyond a charge ratio (+:-) of 2:1, and did not aggregate by the addition of siRNA at any charge ratios (+:-).

To examine the effects of the charge ratio (+:-) of cationic lipoplexes on gene knockdown, MCF-7-Luc cells were incubated with cationic lipoplexes at a final concentration of 50 nM siRNA, and the gene-silencing effect was then assessed by assaying the luciferase activity. LP-OH-C, LP-DOTAP, LP-DC-1-18 and LP-TC-1-12 lipoplexes with Luc siRNA strongly suppressed luciferase activity at any of the charge ratios (+:-) tested (Fig. 2). By contrast, the LP-OH, LP-HAPC and LP-MHAPC lipoplexes with Luc siRNA increased the suppression level of luciferase activity with an increase in the charge ratio (+:-), and exhibited potent suppression of luciferase activity at charge ratios (+:-) of approximately 5:1-7:1 (Fig. 2A). From the results of lipoplex size (Table I) and the gene silencing efficacy by Luc siRNA (Fig. 2), in subsequent experiments, we decided to use cationic lipoplexes formed at charge ratios (+:-) of 7:1 for cationic liposomes composed of cationic cholesterol derivatives and 4:1 for those of dialkyl or trialkyl cationic lipids. Previously, we examined the association of siRNA with each cationic liposomes using an exclusion assay with SYBR^®-Green I, and confirmed that in all the cationic liposomes, the fluorescence of SYBR^®-Green I was markedly decreased by the addition of cationic liposomes into siRNA solution at the above-mentioned charge ratios (+:-) (25).

We have previously reported that PEGylated LP-OH-C lipoplexes modified with 1 mol% PEG₂₀₀₀-DSPE exerted portent in vitro gene silencing effects in MCF-7 cells, as well as non-PEGylated LP-OH-C lipoplexes, and the injection of PEGylated LP-OH-C lipoplexes with siRNA suppressed the expression of a target gene in the liver (14). Furthermore, we found that the PEGylation of LP-OH-C lipoplexes with 2-3 mol% PEG₂₀₀₀-DSPE decreased the in vitro gene silencing effect (unpublished data). Therefore, in this study, we prepared PEGylated liposomes including 1 mol% PEG₂₀₀₀-DSPE into the formulations of cationic liposomes. LP-OH-PEG, LP-OH-C-PEG, LP-HAPC-PEG, LP-MHAPC-PEG, LP-DOTAP-PEG, LP-DC-1-18-PEG and LP-TC-1-12-PEG included 1 mol% PEG₂₀₀₀-DSPE in the formulations of LP-OH, LP-OH-C, LP-HAPC, LP-MHAPC, LP-DOTAP, LP-DC-1-18 and LP-TC-1-12, respectively. The sizes of the PEGylated cationic liposomes were approximately 90-120 nm, and the ζ-potentials were approximately +40-47 mV (Table II). When the liposomes were mixed with siRNA, the lipoplex sizes were approximately 120-170 nm and their ζ-potentials were approximately +32-40 mV (Table II).

To examine the effects of the PEGylation of cationic liposomes on gene knockdown by PEGylated cationic lipoplexes with siRNA, MCF-7-Luc cells were incubated with PEGylated cationic lipoplexes at a 50 nM final concentration of siRNA. As a result, the LP-OH-C-PEG, LP-HAPC-PEG, LP-DOTAP-PEG, LP-DC-1-18-PEG and LP-TC-1-12-PEG lipoplexes with Luc siRNA strongly suppressed luciferase activity (>70% knockdown, compared with Cont siRNA) (Fig. 3), suggesting that the PEGylation did not largely affect the gene silencing effect of the LP-OH-C, LP-HAPC, LP-DOTAP, LP-DC-1-18 and LP-TC-1-12 lipoplexes. By contrast, the LP-OH-PEG and LP-MHAPC-PEG lipoplexes decreased the gene silencing activity by 1 mol% PEGylation (47 and 28% knockdown, respectively, compared with Cont siRNA) (Fig. 3). These results indicated that the inhibition of the gene silencing effect by PEGylation was affected by cationic lipid type in the PEGylated cationic liposomes.

To examine the effects of the type of cationic lipid on cytotoxicity of non-PEGylated and PEGylated cationic lipoplexes, we investigated cell viabilities at 24 h following transfection in the MCF-7 cells with non-PEGylated and PEGylated cationic lipoplexes. The LP-DC-1-18-PEG and non-PEGylated LP-TC-1-12 lipoplexes exhibited slight cytotoxicity (74 and 78%, respectively, in cell viability); however, the other lipoplexes did not exhibit cytotoxicity (Fig. 4).

To prevent the aggregation of cationic lipoplexes with blood components, such as erythrocytes following systemic injection, the modification of the liposome surface with PEG has generally been used. Previously, we reported that 1 mol% PEGylation of LP-OH or LP-OH-C lipoplexes prevented cationic lipoplex-induced agglutination (14). In this study, to examine this effect, non-PEGylated and PEGylated cationic lipoplexes were added into erythrocyte suspensions. Of the non-PEGylated cationic liposomes, all the cationic lipoplexes induced agglutination after mixing with the erythrocyte suspension, regardless of the type of cationic lipid in the liposomal formulation (Fig. 5). In particular, the formation of large-sized aggregates was observed after mixing LP-DOTAP or LP-TC-1-12 lipoplexes with erythrocyte suspensions. In the PEGylated cationic liposomes with cationic cholesterol derivatives, PEG on the surface of cationic lipoplexes prevented agglutination with erythrocyte (Fig. 5). However, in the LP-DOTAP-PEG and LP-DC-1-18-PEG lipoplexes, the formation of small-sized aggregates was observed after the addition of their lipoplexes, indicating that PEGylation could not completely prevent the interaction between cationic lipoplexes and erythrocytes. By contrast, in the LP-TC-1-12-PEG lipoplexes, decreased numbers of erythrocytes were observed following the addition of LP-TC-1-12-PEG lipoplexes into the erythrocyte suspension. LP-TC-1-12-PEG, with short-length trialkyl chains (C12), might induce hemolysis by altering the erythrocyte membrane (26). From this result, LP-TC-1-12-PEG lipoplexes may not be suitable for in vivo transfection.

To examine the effects of PEGylation of cationic liposomes on the biodistribution of siRNA following the intravenous injection of PEGylated cationic lipoplexes, we injected non-PEGylated or PEGylated cationic lipoplexes with Cy5.5-siRNA intravenously into mice and observed the biodistribution of siRNA at 1 h after the injection. In non-PEGylated cationic lipoplexes, the LP-HAPC, LP-DOTAP, LP-DC-1-18 and LP-TC-1-12 lipoplexes largely accumulated mainly in the lungs (Fig. 6), as previously reported (25). By contrast, the LP-OH, LP-OH-C and LP-MHAPC lipoplexes largely accumulated mainly in the liver (25). We have previously reported that differences in the hydrophobic anchor or the length of the alkyl chains of cationic lipids strongly influenced the biodistribution of siRNA after the injection of cationic lipoplexes (25). The injection of cationic lipoplexes with cationic cholesterol derivatives or dialkyl cationic lipids with short dialkyl chains (C12-C14) tended to induce siRNA accumulation in the liver, and those with long dialkyl chains (C16-C18) or with short trialkyl chains (C12) induced siRNA accumulation in the lungs. These findings indicated that siRNA biodistribution after intravenous injection of cationic lipoplexes was strongly affected by the type of cationic lipid in the cationic liposomes. In the PEGylated cationic lipoplexes, the PEGylation of LP-OH, LP-OH-C, LP-HAPC, and LP-MHAPC lipoplexes increased the accumulation of siRNA in the liver (Fig. 6A). Blood components, such as erythrocytes and fibronectin are bound to positively charged lipoplexes in the blood circulation (27). The agglutinates of cationic lipoplexes with erythrocytes contribute to the high entrapment of lipoplexes in highly extended lung capillaries (28). These findings indicated that the PEGylation of cationic lipoplexes could prevent agglutination with erythrocytes in the blood circulation, and lead to an increase in the accumulation of siRNA in the liver. However, in the LP-DOTAP-PEG, LP-DC-1-18-PEG and LP-TC-1-12-PEG lipoplexes, siRNA accumulated mainly in the lungs, suggesting that 1 mol% PEGylation did not largely affect the siRNA biodistribution (Fig. 6B). In the LP-DOTAP-PEG and LP-DC-1-18-PEG lipoplexes, small-sized aggregates of erythrocytes (Fig. 5) may be entrapped in lung capillaries.

In a preliminary experiment, for PEGylated cationic liposomes with dialkyl cationic lipid, we prepared 1, 2, 3 and 5 mol% PEGylated cationic liposomes composed of DOTAP/cholesterol (Chol). We found that 1 mol% PEGylation of cationic lipoplexes prevented the agglutination of erythrocytes by cationic lipoplexes; however, 5 mol% PEGylation was required for cationic liposomes to prevent accumulation of siRNA in the lungs (Fig. S1). This indicated that PEGylated cationic lipoplexes with 1-3 mol% PEG₂₀₀₀-DSPE may accumulate in the lungs without agglutination with erythrocytes. It has been previously reported that 1 mol% PEGylated cationic lipoplexes (AtuFECT01) with asymmetric dialkyl cationic lipids (C16 and C18) selectively target the vasculature in the lungs after systemic injection into mice (15). The PEGylated cationic lipoplexes with dialkyl or trialkyl cationic lipids used in the present study may induce the accumulation of siRNA in the lungs by the direct interaction of the lipoplexes with pulmonary endothelial cells.

To examine the effects of cationic lipid type in PEGylated cationic liposomes on the gene silencing effect of siRNA in mouse liver, we injected PEGylated cationic lipoplexes with ApoB siRNA intravenously into mice to evaluate the knockdown efficiency in the liver. The ApoB gene is a hepatocyte-expressed gene involved in cholesterol transport. Among the PEGylated cationic lipoplexes, PEGylated cationic lipoplexes with cationic cholesterol derivatives induced the accumulation of siRNA in the liver after intravenous injection (Fig. 6A). Previously, we reported that LP-OH-C-PEG lipoplexes containing 1 mol% PEG₂₀₀₀-DSPE significantly suppressed ApoB mRNA levels in the liver, compared with Cont siRNA (approximately 59% knockdown) (14). Therefore, in this study, we evaluated the knockdown efficiency of ApoB mRNA in the liver following the intravenous injection of LP-OH-PEG, LP-HAPC-PEG and LP-MHAPC-PEG lipoplexes with ApoB siRNA. However, the injection of these lipoplexes with ApoB siRNA did not affect the ApoB mRNA levels in the liver (Fig. 7A). Furthermore, in order to evaluate liver toxicity in mice, we assessed the GOT levels in serum at 48 h after the injection of PEGylated cationic lipoplexes. The injection of any of the tested lipoplexes did not significantly elevate the GOT levels in serum (Fig. 7B), indicating that injection of PEGylated cationic lipoplexes had no side-effects with regard to hepatotoxicity, regardless of the type of cationic lipid in the liposomal formulation.

The injection of LP-OH-PEG, LP-HAPC-PEG and LP-MHAPC-PEG lipoplexes with ApoB siRNA did not affect the ApoB mRNA levels in the liver (Fig. 7A), although their lipoplexes accumulated mainly in the liver (Fig. 6A). We speculated that PEG may not be able to completely protect LP-OH-PEG, LP-HAPC-PEG and LP-MHAPC-PEG lipoplexes from protein absorption in the blood circulation, resulting in their capture by Kupffer cells in the liver. However, the mechanisms through which LP-OH-C-PEG lipoplexes suppress the expression of a target gene in the liver are unclear (14). Further studies are required to examine the effects of a cationic cholesterol derivative in PEGylated cationic liposomes on the gene silencing effect of siRNA in the liver following intravenous injection. From the results in this and previous studies (14), LP-OH-C-PEG may have potential as a gene vector for siRNA delivery into the liver.

For evaluation of the gene silencing effect in mouse lungs by PEGylated cationic lipoplexes, we injected PEGylated cationic lipoplexes with Tie2 siRNA intravenously into mice. The Tie2 gene has been used as a marker for vascular endothelium (16). Among the PEGylated cationic lipoplexes, PEGylated cationic lipoplexes with dialkyl or trialkyl cationic lipid induced the accumulation of siRNA in the lungs following intravenous injection (Fig. 6B). Therefore, we used LP-DOTAP-PEG, LP-DC-1-18-PEG and LP-TC-1-12-PEG for the evaluation of the knockdown efficiency in the lungs. As a result, the injection of LP-DC-1-18-PEG lipoplexes with Tie2 siRNA significantly suppressed the Tie2 mRNA levels in the pulmonary endothelium (approximately 45% knockdown), compared with Cont siRNA (Fig. 8). By contrast, the injection of LP-DOTAP-PEG and LP-TC-1-12-PEG lipoplexes with Tie2 siRNA did not affect the mRNA levels compared with Cont siRNA. Previously, we reported that the injection of non-PEGylated LP-DOTAP, LP-DC-1-18, and LP-TC-1-12 lipoplexes with Tie2 siRNA suppressed the Tie2 mRNA levels in the pulmonary endothelium (approximately 19, 74 and 60% knockdown, respectively), compared with those with Cont siRNA (25). LP-TC-1-12-PEG lipoplexes may abolish in vivo gene silencing activity by the PEGylation of cationic liposomes. Among the PEGylated cationic liposomes, LP-DC-1-18-PEG may have potential for use as a gene vector for siRNA delivery into the lungs. From the results of this study, the siRNA biodistribution and in vivo knockdown efficiency following the intravenous injection of PEGylated cationic lipoplexes were strongly affected by the type of cationic lipid in PEGylated cationic liposomes. The selection of cationic lipids in the liposomal formulations may be important for the successful in vivo delivery of siRNA by PEGylated cationic liposomes.

In conclusion, the PEGylation of cationic liposomes generally lowers the efficiency of siRNA-mediated gene silencing in vitro and in vivo. Therefore, in this study, we evaluated whether 1 mol% PEGylation of cationic liposomes could improve the stability of cationic lipoplexes following systemic injection and suppress the expression of a target gene. From the results of this study, the in vivo silencing effects by PEGylated cationic lipoplexes did not closely correspond to the in vitro silencing effects. The siRNA biodistribution and in vivo knockdown efficiency following the intravenous injection of PEGylated cationic lipoplexes were strongly affected by the type of cationic lipid in PEGylated cationic liposomes. This study provides valuable information about the PEGylation of cationic lipoplex for efficient siRNA delivery in vivo.